首页> 外文期刊>African Journal of Microbiology Research >Prevalence and molecular typing of extended-spectrum -lactamases in Escherichia coli, Enterobacter cloacae and Citrobacter freundii isolates from Laghouat Hospital, Algeria
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Prevalence and molecular typing of extended-spectrum -lactamases in Escherichia coli, Enterobacter cloacae and Citrobacter freundii isolates from Laghouat Hospital, Algeria

机译:阿尔及利亚拉古瓦特医院大肠埃希菌,阴沟肠杆菌和弗氏柠檬酸杆菌中广谱内酰胺酶的流行和分子分型

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The antibiotic resistance of enterobacteriacae knows a worldwide worrying evolution with an increase of the extended-spectrum β-lactamases. The present study was to determine the prevalence and molecular typing of extended-spectrum β-lactamases (ESBLs) in clinical isolates of Escherichia coli, Enterobacter cloacae, and Citrobacter freundii, isolated between January 2010 and December 2012, at the Laghouat "Ahemida Ben Adjila" hospital, Algeria. Antimicrobial susceptibility testing was determined by disk diffusion on Mueller Hinton agar. Genetic transfers were performed by conjugation and plasmid DNA was extracted by the alcalin-lysis method. The characterization of ESBL genes were examined using PCR amplification and DNA sequencing and the clonal relatedness was investigated by ERIC-PCR. During the study period, twenty-one (8.23%) isolates were found to produce ESBLs, distributed as follows: 13 isolates of E. coli (61.9%), 6 isolates of E. cloacae (28.57%) and 2 isolates of C. freundii with 9.52 %. The CTX-M-15 ESBL were predominant (95.24%), followed by TEM-4 (14.28%) and SHV-12 (4.76%). ERIC-PCR analysis showed that the isolates are genetically unrelated and conjugation experiments showed that blaCTX-M-15 gene was transferred on a conjugative plasmid of high molecular weight (≈130 kb). This study indicated a high prevalence of CTX-M-15 enzymes among E. coli, E. cloacae and C. freundii in Laghouat hospital, Algeria.
机译:肠杆菌的抗生素耐药性随着广谱β-内酰胺酶的增加而在世界范围内引起人们的担忧。本研究旨在确定2010年1月至2012年12月在Laghouat“ Ahemida Ben Adjila阿尔及利亚的医院。通过在Mueller Hinton琼脂上进行圆盘扩散来确定抗菌药敏试验。通过缀合进行遗传转移,并通过alcalin裂解法提取质粒DNA。使用PCR扩增和DNA测序检查ESBL基因的特征,并通过ERIC-PCR研究克隆的相关性。在研究期间,发现二十一种(8.23%)分离物可产生ESBL,分布如下:大肠杆菌13株(61.9%),阴沟肠杆菌6株(28.57%)和2株隐球菌。 freundii,占9.52%。 CTX-M-15 ESBL占主导地位(95.24%),其次是TEM-4(14.28%)和SHV-12(4.76%)。 ERIC-PCR分析表明分离物在遗传上不相关,结合实验表明blaCTX-M-15基因已转移到高分子量(≈130kb)的结合质粒上。这项研究表明在阿尔及利亚拉古瓦特医院,大肠杆菌,阴沟肠杆菌和弗氏梭状芽胞杆菌中CTX-M-15酶的患病率很高。

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